Method for enhancing mutant enzyme activities in Gaucher disease

ABSTRACT

Method for enhancing in a mammalian cell the activity of an enzyme associated with Gaucher Disease by administering a competitive inhibitor of glucocerebrosidase in an amount effective to enhance the activity of the enzyme. Preferred compounds for use in the method are imino sugars and related compounds. In particular, C8–12-alkyl derivatives of N-alkyl-deoxynojirimycin, isofagomine compounds, and calystegine compounds are effective to enhance glucocerebrosidase activity.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is a continuation of application Ser. No. 10/304,395 filed Nov. 26, 2002, now U.S. Pat. No. 6,916,829, which is a continuation of application Ser. No. 09/948,348, filed Sep. 7, 2001, now U.S. Pat. No. 6,599,919, which is a continuation of application Ser. No. 09/604,053, filed Jun. 26, 2000, now U.S. Pat. No. 6,583,158, which is a continuation-in-part of application Ser. No. 09/087,804, filed Jun. 1, 1998, now U.S. Pat. No. 6,274,597. Each of these prior references in hereby incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a method of enhancing mutant enzyme activities in lysosomal storage disorders by administration of competitive inhibitors of the enzymes, in particular, imino sugars and related compounds.

2. Background Information

Proteins are synthesized in the cytoplasm, and the newly synthesized proteins are secreted into the lumen of the endoplasmic reticulum (ER) in a largely unfolded state. In general, protein folding is an event governed by a principle of self assembly. The tendency of proteins to fold into their native (active) conformation is contained in their amino acid sequences (1). In vitro, the primary structure folds into secondary structres of α-helices and β-sheets coupled with hydrophobic collapse in the formation of biologically active tertiarystructure which also gains increased conformational stability. However, the folding of protein in vivo is rather complicated, because the combination of ambient temperature and high protein concentration stimulates the process of aggregation, in which amino acids normally buried in the hydrophobic core interact with their neighbors non-specifically. To avoid this problem, protein folding is usually facilitated by a special group of proteins called molecular chaperones which prevent nascent polypeptide chains from aggregating, and bind to protein so that the protein refolds in the active state (2).

Molecular chaperones are present in virtually all types of cells and in most cellular compartments. Some are involved in the transport of proteins and in supporting cells to survive under stresses such as heat shock and glucose starvation. Among the molecular chaperones (3–6), BIP (immunoglobulin heavy-chain binding protein, Grp78) is the best characterized chaperone of the ER (7). Like other molecular chaperones, BIP interacts with many secretory and membrane proteins within the ER throughout their maturation, although the interaction is normally weak and short-lived when the folding proceeds smoothly. Once the native protein conformation is achieved, the molecular chaperone no longer binds. However, the interaction between BIP and those proteins that fail to fold, assemble or be properly glycosylated becomes stable, and usually leads to degradation of these proteins through the ubiquitin pathway. This process serves as a “quality control” system in the ER which ensures that only properly folded and assembled proteins are transported to the Golgi complex for further maturation, and those improperly folded proteins are retained for subsequent degradation (8).

In many hereditary disorders, mutant gene products are structurally altered and may not fold correctly, signalling the quality control system to retain and degrade them in situ. This process may contribute significantly to the protein deficiency, although the function of the protein may have been only partially impaired (9–12). For example, the most common mutation in cystic fibrosis, a deletion of phenylalanine-508 (ΔF508) in the CFTR protein which functions as a chloride channel in the plasma membrane, results in misfolding and retardation of the ΔF508-CFTR protein in the ER, and subsequent degradation by the cytosolic proteasome system (13–14), even though it retains almost full biologic activity when inserted into plasma membranes (15). The list of diseases caused by mutations that alter protein folding is increasing, and it includes α₁-antitrypsin deficiency (16–17), familial hypercholesterolemia (18), Alzheimer's disease (18a), Marfan syndrome (19), osteogenesis imperfecta (20), carbohydrate-deficient glycoprotein syndrome (21), and Maroteaux-Lamy syndrome (22).

Lysosomal storage disorders are a group of diseases resulting from the abnormal metabolism of various substrates, including glycosphingolipids, glycogen, mucopolysaccharides and glycoproteins. The metabolism of exo- and endogenous high molecular weight compounds normally occurs in the lysosomes, and the process is normally regulated in a stepwise process by degradation enzymes. Therefore, a deficient activity in one enzyme may impair the process, resulting in an accumulation of particular substrates. Most of these diseases can be clinically classified into subtypes: i) infantile-onset; ii) juvenile-onset; or iii) late-onset. The infantile-onset forms are often the most severe usually with no residual enzyme activity. The later-onset forms are often milder with low, but often detectable residual enzyme activity. The severity of the juvenile-onset forms are in between the infantile-onset and late-onset forms. Table 1 contains a list of a number of known lysosomal storage disorders and their associated defective enzymes. In the adult-onset forms of lysosomal storage disorders listed in Table 1, certain mutations cause instability of the encoded protein.

TABLE 1 Lysosomal storage disorders. Lysosomal storage disorder Defective enzyme Pompe disease Acid α-glucosidase Gaucher disease Acid β-glucosidse, or glucocerebrosidase Fabry disease α-Galactosidase A G_(M1)-gangliosidosis Acid β-galactosidase Tay-Sachs disease β-Hexosaminidase A Sandhoff disease β-Hexosaminidase B Niemann-Pick disease Acid sphingomyelinase Krabbe disease Galactocerebrosidase Farber disease Acid ceramidase Metachromatic Arylsulfatase A leukodystrophy Hurler-Scheie disease α-L-Iduronidase Hunter disease Iduronate-2-sulfatase Sanfilippo disease A Heparan N-sulfatase Sanfilippo disease B α-N-Acetylglucosaminidase Sanfilippo disease C Acetyl-CoA: α-glucosaminide N- acetyltransferase Sanfilippo disease D N-Acetylglucosamine-6-sulfate sulfatase Morquio disease A N-Acetylgalactosamine-6-sulfate sulfatase Morquio disease B Acid β-galactosidase Maroteaux-Lamy disease Arylsulfatase B Sly disease β-Glucuronidase α-Mannosidosis Acid α-mannosidase β-Mannosidosis Acid β-mannosidase Fucosidosis Acid α-L-fucosidase Sialidosis Sialidase Schindler-Kanzaki disease α-N-acetylgalactosaminidase

In their earlier filed patent application (U.S. application Ser. No. 09/087,804), the present inventors proposed a novel therapeutic strategy for Fabry disease, a lysosomal storage disorder caused by deficient lysosomal α-galactosidase A (α-Gal A) activity in which certain mutations encoded mutant proteins which have folding defects. The application presented evidence demonstrating that 1-deoxygalactonojirimycin (DGJ), a potent competitive inhibitor of α-Gal A, effectively increased in vitro stability of a mutant α-Gal A (R301Q) at neutral pH and enhanced the mutant enzyme activity in lymphoblasts established from Fabry patients with the R301Q or Q279E mutations. Furthermore, oral administration of DGJ to trangenic mice overexpressing a mutant (R301Q) α-Gal A substantially elevated the enzyme activity in major organs (24).

The principle of this strategy is as follows. Since the mutant enzyme protein appears to fold improperly in the ER where pH is neutral, as evidenced by its instability at pH 7 in vitro (25), the enzyme protein would be retarded in the normal transport pathway (ER→Golgi apparatus→endosome→lysosome) and subjected to rapid degradation. In contrast, an enzyme protein with a proper folding conformation could be efficiently transported to the lysosomes and remain active, because the enzyme is more stable below pH 5. Therefore, a functional compound which is able to induce a stable molecular conformation of the enzyme is expected to serve as a “chemical chaperone” for the mutant protein to stabilize the mutant protein in a proper conformation for transport to the lysosomes. Some inhibitors of an enzyme are known to occupy the catalytic center of enzyme, resulting in stabilization of its conformation in vitro, they may also serve as “chemical chaperones” to enforce the proper folding of enzyme in vivo, thus rescue the mutant enzyme from the ER quality control system. It is noted that while this is believed to be the mechanism of operation of the present invention, the success of the invention is not dependent upon this being the correct mechanism.

SUMMARY OF THE INVENTION

The present inventors have unexpectedly found that potent competitive inhibitors for enzymes associated with lysosomal storage disorders enhance the activity of such enzymes in cells when administered at concentrations lower than that normally required to inhibit the intracellular enzyme activity. The effect is particularly significant on certain defective or mutant enzymes, but also occurs in cells containing the normal enzyme type.

Accordingly, it is one object of the present invention to provide a method of preventing degradation of mutant enzymes associated with lysosomal storage diseases in mammalian cells, particularly in human cells.

It is a further object of the invention to provide a method of enhancing the activity of enzymes associated with lysosomal storage disease in mammalian cells, particularly in human cells. The method of the present invention enhance the activity of both normal and mutant α-Gal A, particularly of mutant α-Gal A which is present in certain forms of Fabry disease. The methods of the present invention also enhance the activity of certain mutant β-galactosidase and glucocerebrosidase and are expected to be useful in other lysosomal storage diseases, including those listed in Table 1.

In addition, the methods of the invention are also expected to be useful in nonmammalian cells, such as, for example, cultured insect cells and CHO cells which are used for production of α-Gal A for enzyme replacement therapy.

It is yet a further object of the invention to provide a method of treatment for patients with lysosomal storage disorders such as those listed in Table 1.

Compounds expected to be particularly effective for Fabry disease in the methods of the invention are galactose and glucose derivatives having a nitrogen replacing the oxygen in the ring, preferably galactose derivatives such as 1-deoxygalactonojirimycin and 4-epi-α-homonojirimycin. The term “galactose derivative” is intended to mean that the hydroxyl group at the C-3 position is equatorial and the hydroxyl group at the C-4 position is axial, as represented, for example, by the following structures:

wherein R₀ represents H, methyl or ethyl; R₁ and R₁′ independently represent H, OH, a 1–4 carbon alkyl alkoxy or hydroxyalkyl group (e.g., CH₂OH); R₂ and R₂′ independently represent H, OH or alkyl group (n=1–8).

Other specific competitive inhibitors for α-galactosidase such as for example, calystegine A₃ and B₂, and N-methyl derivatives of these compounds should be useful in the method of the invention. The calystegine compounds can be represented by the formula

wherein for calystegine A₃: R₀=H, R₂=R₂′=H; R₄=OH, R₄′=R₇=H; for calystegine B₂: R₀=H, R₂=OH, R₂′=R₄′=H, R₄=OH, R₇=H; for N-methyl-calystegine A₃: R₀=CH₃, R₂′=H, R₄=OH, R₄′=R₇=H; for N-methyl-calystegine B₂: R₀=CH₃, R₂=OH, R₂′=H, R₄=OH, R₇=H.

Administration of a pharmaceutically effective amount of a compound of formula

wherein R₀ represents H, methyl or ethyl; R₁ and R_(1′) independently represent H, OH, a 1–4 carbon alkyl, alkoxy or hydroxyalkyl group (e.g., CH₂OH); R₂ and R₂′ independently represent H, OH or alkyl group (n=1–8); R₄ and R₄′ independently represent H, OH; or a compound selected from the group consisting of α-allo-homonojirimycin, α-galacto-homonojirimycin, β-1-C-butyl-deoxygalactonojirimycin, calystegine A₃, calystegine B₂ and their N-alkyl derivatives will alleviate the symptoms of Fabry disease by increasing the residual enzyme activity in patients suffering from Fabry disease.

Compounds expected to be particularly effective for G_(M1)-gangliosidosis in the methods of the invention are galactose derivatives having a nitrogen replacing the oxygen in the ring or a nitrogen at the same position of the anomeric position of a pyranose ring, preferably galactose derivatives such as 4-epi-isofagomine and 1-deoxygalactonojirimycin.

Administration of a pharmaceutically effective amount of a compound of formula

wherein R₀ represents H, methyl or ethyl; R₁ R₁′ independently represents H, OH, a 1–4 carbon alkyl, alkoxy or hydroxyalkyl group (e.g., CH₂OH); R₂ and R₂′ independently represent H, OH or alkyl group (n=1–8); or a compound selected from the group consisting of 4-epi-isofagomine and 1-deoxygalactonojirimycin and their N-alkyl derivatives will alleviate the symptoms of G_(M1)-gangliosidosis by increasing the residual β-galactosidase activity in patients suffering from G_(M1)-gangliosidosis.

Compounds expected to be particularly effective for Gaucher disease in the methods of the invention are glucose derivatives having a nitrogen replacing the oxygen in the ring or a nitrogen at the same position of the anomeric position of a pyranose ring, preferably glucose derivatives such as N-dodecyl-deoxynojirimycin and isofagomine. The term “glucose derivative” is intended to mean that the hydroxyl groups at the C-3 and C-4 positions are equatorial as represented, for example, by the following structures:

wherein R₀ represents H, alkyl chain (n=8–12); R₀′ represents H, a straight chain or branched saturated or unsaturated carbon chain containing 1–12 carbon atoms, optionally substituted with a phenyl, hydroxyl or cyclohexyl group; R₁ and R₁′ independently represent H, OH, a 1–4 carbon alkyl, alkoxy or hydroxyalkyl group (e.g., CH₂OH); R₂ and R₂′ independently represent H, OH or alkyl group (n=1–8).

Other specific competitive inhibitors for β-glucosidase, such as for example, calystegine A₃, B₁, B₂ and C₁, and their derivatives of these compounds should be useful in the method of the invention. The calysteginic compounds can be represented by the formula

wherein for calystegine A₃: R₀=H, R₂=R₂′=H, R₄=OH, R₄′=R₇=H; for calystegine B₁: R₀=H, R₂=R₂=R₄′=H, R₄=OH, R₇=OH; for calystegine B₂: R₀=H, R₂=OH, R₂′=R₄′=H, R₄=OH, R₇=H; for calystegine C₁: RF=H, R₂=OH, R₂′=H, R₄=OH, R₄′=H, R₇=OH.

Administration of a pharmaceutically effective amount of a compound of formula

wherein R₀ represents H, alkyl chain (n=8–12); R₀′ represents H, a straight chain or branched saturated or unsaturated carbon chain containing 1–12 carbon atoms, optionally substituted with a phenyl, hydroxyl or cyclohexyl group; R₁ and R₁′ independently represent H, OH, a 1–4 carbon alkyl, alkoxy or hydroxyalkyl group (e.g., CH₂OH); R₂ and R₂′ independently represent 1–1, OH or alkyl group (n=1–8); or a compound selected from the group consisting of isofagomine, N-butyl-isofagomine, N-(3-cyclohexylpropyl)-isofagomine, N-(3-phenylpropyl)-isofagomine and N-|(2E,6Z,10Z)-3,7,11-trimethyldodecatrienyl|-isofagomine. N-dodecyl-deoxynojirimycin will alleviate the symptoms of Gaucher disease by increasing the residual glucocerebrosidase activity in patients suffering from Gaucher disease. Other competitive inhibitors of glucocerebrosidase, such as calystegine compounds and N-alkyl derivatives thereof should also be useful for treating Gaucher disease. Similarly, known competitive inhibitors of other enzymes associated with lysosomal storage disorders listed in Table 1 will be useful in treating those disorders.

Persons of skill in the art will understand that an effective amount of the compounds used in the methods of the invention can be determined by routine experimentation, but is expected to be an amount resulting in serum levels between 0.01 and 100 μM, preferably between 0.01 and 10 μM, most preferably between 0.05 and 1 μM. The effective dose of the compounds is expected to be between 0.5 and 1000 mg/kg body weight/day, preferably between 0.5 and 100 mg/kg body weight/day, most preferably between 1 and 50 mg/kg body weight/day. The compounds can be administered alone or optionally along with pharmaceutically acceptable carriers and excipients, in preformulated dosages. The administration of an effective amount of the compound will result in an increase in the lysosomal enzymatic activity of the cells of a patient sufficient to improve the symptoms of the disease.

In many lysosomal storage diseases, much of the clinical variability and age of onset can be attributed to small differences in the residual activity of the affected enzyme (25a). Pseudodeficiency of lysosomal storage disorders identified as clinically healthy probands with severely reduced activity (10–20% of normal) of a lysosomal enzyme suggests that a small increase of residual enzyme activity could have a large effect on the disease (25b). Particularly in Fabry disease, a small augmentation in enzyme stability resulting in an increase of residual α-Gal A activity is expected to have a significant impact on the disease, based on the observations on the cardiac variants with 10% residual activity (2). Therefore, a small percentage increase of the residual enzyme activity may alleviate symptoms of the disease or significant delay the development of the disease.

Compounds disclosed herein and other competitive inhibitors of enzymes associated with lysosomal storage diseases which will be known to those of skill in the art will be useful according to the invention in methods of enhancing the intracellular activity of normal and mutant enzymes associated with such disorders and treating the disorders.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Structures of inhibitors used in this study.

The numbering of carbons for compounds 2–6, 11–16, 30–32 is the same as in compound 1; the numbering of carbons for compounds 8–10 is the same as in compound 7; the numbering of carbons for compounds 18–20, 22–26 is the same as in compound 17; the numbering of carbons for compounds 33–37 is the same as in compound 21.

FIG. 2. Stereostructure of α-allo-HNJ (9).

A and B are identical, but viewed from different angles. C is a proposed stereo-structure for α-allo-HNJ (9) deduced from NMR analysis. D is a presumed reaction intermediate for α-galactosidase.

FIG. 3. Lineweaver-Burk plots of DGJ (4) (A), α-allo-HNJ (9) (B), α-galacto-HNJ (10) (C), and β-1-C-butyl-DGJ (16) (D) inhibition of α-Gal A.

The increasing concentrations of substrate were used to determine the K_(m) and K_(i) values and the data were plotted as 1/v vs. 1/S. The calculated K_(m) for p-nitrophenyl-α-D-galactopyranoside was 0.17 mM. (A) Concentrations of 4 were 0 (●), 0.1 μM (▴), and 0.25 μM (▪). The calculated K_(i) value was 0.04 μM. (B) Concentrations of 9 were 0 (●), 2.5 μM (▴), and 5 μM (▪). The calculated K_(i) value was 2.6 μM. (C) Concentrations of 10 were 0 (●), 0.1 μM (▴), and 0.25 μM (▪). The calculated K_(i) value was 0.17 μM. (D) Concentrations of 16 were 0 (●), 10 μM (▴), and 25 μM (▪). The calculated K_(i) value was 16 μM.

FIG. 4. In vitro inhibition (A) and intracellular enhancement (B) of α-Gal A by inhibitors.

(A) Concentrations for 50% inhibition of α-Gal A (IC₅₀) were determined with p-nitrophenyl-α-D-galactopyranoside as the substrate. (B) Each inhibitor was added to the culture medium of R301Q lymphoblasts at a concentration of 100 μM. Cells were subsequently incubated for 4 days. After being washed twice with phosphate-buffered saline, the intracellular enzyme activity was determined with 4-MU-α-Gal as the substrate.

FIG. 5. Effect of the increasing concentrations of selected inhibitors on α-Gal A activity.

R301Q lymphoblasts were cultured with DGJ (4) (●), α-allo-HNJ (9) (▪), α-galacto-HNJ (10) (▴), or β-1-C-butyl-DGJ (16) (♦) at 1–1000 μM for 4 days before being collected for enzyme assay.

FIG. 6. Intracellular enhancement of α-Gal A activity in Fabry lymphoblasts by calystegine compounds.

R301Q lymphoblasts were cultured with calystegine A₃ (17) (A), calystegine B₂ (18) (B), N-methyl calystegine A₃ (19) (C), or N-methyl calystegine B₂ (20) (D) at 100–1000 μM for 4 days before being collected for enzyme assay.

FIG. 7. Intracellular enhancement of β-Gal activity in G_(M1)-gangliosidosis fibroblasts.

A, G_(M1)-gangliosidosis fibroblasts were cultured with DGJ (4) at 500 μM for 5 days before being collected for enzyme assay. B, G_(M1)-gangliosidosis fibroblasts were cultured with 4-epi-isofagomine (21) at 50 μM for 5 days before being collected for enzyme assay. Strains BGF-1 and BGF-6 were diagnosed as infantile type, and all others were juvenile or adult types.

FIG. 8. Intracellular enhancement of β-Glu activity in Gaucher fibroblasts by isofagomine (33).

A, Gaucher fibroblasts (N370S/N370S) were cultured with isofagomine (33) at 1–100 μM for 5 days before being collected for enzyme assay. B, Time course of intracellular enhancement of β-Glu activity in Gaucher cells by isofagomine.

FIG. 9. Intracellular enhancement of β-Glu activity in Gaucher fibroblasts by isofagomine derivatives. Gaucher fibroblasts (N370S/N370S) were cultured with isofagomine derivatives (34–37) at 10 or 100 μM for 5 days before being collected for enzyme assay.

FIG. 10. Intracellular enhancement of β-Glu activity in Gaucher fibroblasts by dodecyl-DNJ (31).

A, Gaucher fibroblasts (N370S/N370S) were cultured with dodecyl-DNJ (31) at 0.05–5 μM for 5 days before being collected for enzyme assay. B, Time course of intracellular enhancement of β-Glu activity in Gaucher cells cultured in the presence (∘) or absence (●) of dodecyl-DNJ.

FIG. 11. Intracellular enhancement of β-Glu activity in Gaucher fibroblasts by calystegine compounds. Gaucher fibroblasts (L444P/L444P) were cultured with calystegine compounds (17, 18, 23 and 26) at 1–100 μM for 5 days before being collected for enzyme assay. A, calystegine B₂ (18); B, calystegine B₁ (23); C, calysteginc A₃ (17); and D, calystegine C₁ (26).

FIG. 12. Structure of iminosugars

DETAILED DESCRIPTION OF THE INVENTION

In the work leading to the present application, the inventors tested a series of naturally occurring and chemically synthesized novel inhibitors for both in vitro inhibition of normal α-Gal A and intracellular enhancement of a mutant a α-Gal A activity with Fabry lymphoblasts to demonstrate that potent competitive reversible inhibitors of α-Gal A are effective “chemical chaperones” which can stabilize the mutant enzyme and rescue it from degradation. Applicants now have tested the chemical chaperone strategy with Gaucher disease and G_(M1)-gangliosidosis, both of which belong to the lysosomal storage disorder family (26–27), to demonstrate that this therapeutic strategy of using potent competitive inhibitors as chemical chaperones to enhance the residual enzyme activity in the patient's cells is not limited to Fabry disease, and can be applied to Gaucher disease and G_(M1)-gangliosidosis as examples of the principle which can be extended to to other lysosomal storage disorders as listed in Table 1.

Materials and Methods

Inhibitors the Structures of the Inhibitors Used in this Invention are Shown in FIG. 1.

1-deoxynojirimycin (DNJ) (1) was isolated from the roots of Morus alba (Moraceae) as described previously (28). 1-Deoxymannojirimycin (manno-DNJ) (2) and 1-deoxy-3,4-diepi-nojirimycin (gulo-DNJ) (5) have been recently isolated from the barks of Angylocalyx pynaertii (Leguminosae). 1-Deoxy-3-epi-nojirimycin (allo-DNJ) (3) was prepared by the microbial redox reaction at C-3 of the N-benzyloxycarbonyl derivative of DNJ as described previously (29). 1-Deoxygalactonojirimycin (DGJ) (4) and 1,2-dideoxy-galactonojirimycin (6) were prepared by the chemical epimerization of the 4-OH group of 1 and fagomine, respectively, according to the literature procedure (30). α-Homonojirimycin (α-HNJ) (7), α-homomannojirimycin (α-manno-HNJ) (8), and α-homoallonojirimycin (α-allo-14NJ) (9) were isolated from the whole plant of Aglaonema tretibii (Araceae) as reported previously (31). α-Homogalactonojirimycin (α-galacto-HNJ) (10) was prepared from 2,3,4,6-tetra-O-benzyl-D-galactose by way of a Wittig chain extension and a mercuricyclization according to the literature procedure (33). N-Methyl-DGJ (11) was prepared by treatment of 4 with 37% HCHO and 80% formic acid according to the reference (34), and the N-ethyl (12), N-propyl (13), N-butyl (14) and N-hydroxyethyl (15) derivatives of 4 were prepared by treatment with the appropriate alkyl bromide and triethylamine in DMF. The reaction mixture of N-alkylation was evaporated in vacuo, and the residual syrup was resolved in MeOH and applied to an Amberlyst 15 column (H⁺form), washed with MeOH, eluted with 0.5 M NH₄OH, and concentrated. N-Alkylated derivatives were finally purified by Dowex 1X2 (OH⁻ form) and Amberlite CG-50 (NH₄ ⁺ form) chromatography with water as eluent. β-1-C-Butyl-DGJ (16) was isolated from Adenophorae Radix as described previously (35). 4-epi-isofagomine (21), isofagomine (33) and its derivatives (34–37) were chemically synthesized as described previously (40). 2,5-Dideoxy-2,5-imino-D-mannitol (DMDP, 27), 1,4-dideoxy-1,4-imino-D-arabinitol (DAB, 28) were purified from Derris malaccensis and Morus alba, respectively (29). N-butyl-DNJ (30), N-dodecyl-DNJ (31), castanospermine (29) were from commercial sources. Calystegine A₃ (17), calystegine A₅ (22), calystegine B₁ (23), calystegine B₂ (18), calystegine B₃ (24), calystegine B₄ (25), and calystegine C₁ (26) were prepared as published method (36, 40a), N-methyl calystegine A₃ (19) and N-methyl calystegine B₂ (20) were chemically synthesized.

Structural characterization of some inhibitors The structural characterization of the inhibitors is determined by mass spectrometry and ¹³C-NMR, and some of the results are presented below.

1-Deoxynojirimycin (DNJ) (1) HRFABMS m/z 164.0923 [M+H]⁺ (C₆H₁₄NO₄ requires 164.0923). ¹³C-NMR (100 MHz, D₂O) δ(ppm downfield from internal sodium 3-(trimethylsilyl)propionate) 51.5 (C-1), 63.3 (C-5), 64.2 (C-6), 73.7 (C-2), 74.3 (C-4), 81.2 (C-3).

1-Deoxymannojirimycin (manno-DNJ) (2) HRFABMS m/z 164.0923 [M+H]⁺ (C₆H₁₄NO₄ requires 164.0923). ¹³C-NMR (100 MHz, D₂O) δ51.5 (C-1), 63.4 (C-5), 63.7 (C-6), 71.3 (C-4), 72.1 (C-2), 77.5 (C-3).

1-Deoxy-3-epi-nojirimycin (allo-DNJ) (3) HRFABMS m/z 164.0922 [M+H]⁺ (C₆H₁₄NO₄ requires 164.0923). ¹³C-NMR (100 MHz, D₂O) δ46.9 (C-1), 59.2 (C-5), 60.7 (C-6), 72.7(C-2), 73.3 (C-4), 75.0 (C-3).

1-Deoxygalactonojirimycin (DGJ) (4) HRFABMS m/z 164.0921 [M+H]⁺ (C₆H₁₄NO₄ requires 164.0923). ¹³C-NMR (100 MHz, D₂O) δ51.9 (C-1), 61.7 (C-5), 64.2 (C-6), 70.9 (C-2), 72.1 (CA4), 77.9 (C-3).

1-Deoxy-3,4-diepi-nojirimycin (gulo-DNJ) (5) HRFABMS m/z 164.0921 [M+H]⁺ (C₆H₁₄NO₄ requires 164.0923). ¹³C-NMR (100 MHz, D₂O) δ46.9 (C-1), 56.9 (C-5), 63.8 (C-6), 68.3 (C-2), 72.0 (CA4), 73.0 (C-3).

1,2-Dideoxygalactonojirimycin (6) HRFABMS m/z 148.0972 [M+H]⁺ (C₆H₁₄NO₃ requires 148.0974). ¹³C-NMR (100 MHz, D₂O) δ30.2 (C-2), 45.6 (C-1), 61.8 (C-5), 64.5 (C-6), 70.5 (C-4), 72.7 (C-3).

α-Homonojirimycin (α-HNJ) (7) HRFABMS m/z 194.1025 [M+H]⁺ (C₇H₁₆NO₅ requires 194.1028). ¹³C-NMR (100 MHz, D₂O) δ56.9 (C-5), 59.1 (C-1′), 59.7 (C-1), 64.8 (C-6), 74.4 (C-2), 74.9 (C-4), 77.1 (C-3).

α-Homomannojirimycin (α-manno-HNJ) (8) HRFABMS m/z 194.1026 [M+H]⁺ (C₇H₁₆NO₅ requires 194.1028). ¹³C-NMR (100 MHz, D₂O) δ58.6 (C5), 61.4 (C-1), 62.2 (C-1′), 63.9 (C-6), 71.4 (C-4), 71.6 (C-2), 74.7 (C-3).

α-Homoallonojirimycin (α-allo-HNJ) (9) HRFABMS m/z 194.1024 [M+H]⁺ (C₇H₁₆NO₅ requires 194.1028). ¹³C-NMR (100 MHz, D₂O) δ57.2 (C-5), 58.1 (C-1), 62.7 (C-1′), 63.5 (C-6), 72.0 (C-4), 72.1 (C-3), 72.2 (C-2).

α-Homogalactonojirimycin (α-galacto-HNJ) (10) HRFABMS m/z 194.1028 [M+H]⁺ (C₇H₁₆NO₅ requires 194.1028). ¹³C-NMR (100 MHz, D₂O) δ55.8 (C-5), 59.3 (C-1), 59.6 (C-1′), 64.5 (C-6), 71.8 (C-2), 71.9 (C-4), 73.8 (C-3).

N-Methyl-1-deoxygalactonojirimycin (N-Me-DGJ) (11) HRFABMS m/z 178.1081 [M+H]⁺ (C₇H₁₆NO₄ requires 178.1079). ¹³C-NMR (100 MHz, D₂O) δ44.2 (N—CH₃), 62.9 (C-1), 63.6 (C-6), 68.5 (C-2), 69.7 (C-5), 73.0 (C-4), 77.8 (C-3).

N-Ethyl-1-deoxygalactonojirimycin (N-Et-DGJ) (12) HRFABMS m/z 192.1237 [M+H]⁺ (C₈H₁₈NO₄ requires 192.1236). ¹³C-NMR (100 MHz, D₂O) δ10.7, 48.9 (N-ethyl), 57.8 (C-1), 63.2 (C-6), 65.0 (C-5), 69.9 (C-2), 73.0 (C-4), 77.9 (C-3).

N-Propyl-1-deoxygalactonojirimycin (N-Pr-DGJ) (13) HRFABMS m/z 206.1392 [M+H]⁺ (C₉H₂₀NO₄ requires 206.1392). ¹³C-NMR (100 MHz, D₂O) δ13.9, 19.2, 57.2 (N-propyl), 58.6 (C-1), 63.3 (C-6), 65.5 (C-5), 69.9 (C-2), 73.0 (C-4), 77.9 (C-3).

N-Butyl-1-deoxygalactonojirimycin (NV-Bu-DGJ) (14) HRFABMS m/z 220.1546 [M+H]⁺ (C₁₀H₂₂NO₄ requires 220.1549). ¹³C-NMR (100 MHz, D₂O) δ16.1, 23.0, 27.9, 55.0 (N-butyl), 58.6 (C-1), 63.3 (C-6), 65.5 (C-5), 69.9 (C-2), 73.0 (C-4), 77.9 (C-3).

N-Hydroxyethyl-1-deoxygalactonojirimycin (N-HE-DGJ) (15) HRFABMS ma/z 208.1183 [M+H]⁺ (C₈H₁₈NO₅ requires 208.1185). ¹³C-NMR (100 MHz, D₂O) δ56.0 (N—CH₂—), 59.2 (C-1), 60.9 (N—CH₂CH₂OH), 63.7 (C-6), 66.4 (C-5), 69.7 (C-2), 73.3 (C-4), 77.8 (C-3).

β-1-C-Butyl-deoxygalactonojirimycin (16) HRFABMS m/z 220.1543 [M+H]⁺ (C₁₀H₂₂NO₄ requires 220.1549). ¹³C-NMR (100 MHz, D₂O) δ16.1, 25.0, 29.6, 33.5 (C-butyl), 61.1 (C-5), 61.8 (C-1), 64.2 (C-6), 71.8 (C-4), 74.9 (C-2), 77.9 (C-3).

Enzyme and in vitro enzyme assay α-Gal A was expressed from Sf-9 insect cells infected with a recombinant baculovirus encoding normal α-Gal A gene and purified to homogeneity by concanavalin A-Sepharose and Mono Q (Pharmacia LKB Biotechnology, Uppsala, Sweden) column chromatography according to the published methods (37). The enzyme activity was assayed with 2 mM p-nitrophenyl-α-D-galactoside as substrate in the presence of bovine serum albumin (3 mg/ml) at pH 4.5.

Cell culture The Epstein-Barr virus-transformed lymphoblast lines from a normal adult and a Fabry patient with R301Q mutation in α-Gal A (38) were cultured in RPMI-1640 medium (Nissui Pharmaceutical Co., Tokyo, Japan) supplemented with 10% fetal calf serum (FCS) at 37° C. under 5% CO₂. Human fibroblasts from Gaucher and G_(M1)-gangliosidosis patients were cultured in McCoy 5A medium supplemented with 10% FCS at 37° C. under 5% CO₂.

Intracellular α-Gal A assay Cells were cultured in the presence or absence of inhibitor for 4 days. After being washed twice with phosphate-buffered saline (PBS), the cells were harvested and homogenized in 200 μl of H₂O, and 10 μl of the supernatant obtained by centrifugation at 10,000 g was incubated at 37° C. with 50 μl of the substrate solution composed by 6 mM 4-methylumbelliferyl α-D-galactoside (4-MU-α-Gal) and 90 mM N-acetylgalactosamine in 0.1 M citrate buffer (pH 4.5) for enzyme assay. One unit of intracellular enzyme activity was defined as one nmol of 4-methylumbelliferone released per hour at 37° C.

Intracellular β-galactosidase assay Cells were cultured in the presence or absence of inhibitor for 5 days. After being washed twice with PBS, the cells were harvested and homogenized in 200 μl of H₂O, and 10 μl of the supernatant obtained by centrifugation at 10,000 g was incubated at 37° C. with 50 μl of the substrate solution of 1 mM 4-methylumbelliferyl β-D-galactoside (4-MU-β-Gal) in 0.1 M citrate buffer (pH 4.5) for enzyme assay. One unit of intracellular enzyme activity was defined as one nmol of 4-methylumbelliferone released per hour at 37° C.

Intracellular glucocerebrosidase assay Cells were cultured in the presence or absence of inhibitor for 5 days. After being washed twice with PBS, the cells were harvested and homogenized in 200 μl of buffer 1 composed by 0.25% sodium taurocholate, 0.1% Triton X-100 and 0.1 M citrate buffer (pH 5.2). The supernatant (10 μl) obtained by centrifugation at 10,000 g was incubated at 37° C. with 50 μl of the substrate solution of 3 mM 4-methylumbelliferyl β-D-glucoside (4-MU-β-Glu) in the buffer 1 for determination of total β-glucosidase activity. The neutral β-glucosidase activity was determined by performing the same assay except pre-incubation of the enzyme solution with 3 mM conduritol B epoxide (an irreversible inhibitor of acid β-Glu) at room temperature for 30 min. The glucocerebrosidase activity was determined by subtracting the neutral β-glucosidase activity from the total enzyme activity. One unit of intracellular enzyme activity was defined as one nmol of 4-methylumbelliferone released per hour at 37° C.

EXAMPLE 1

In Vitro Inhibition and Intracellular Enhancement of α-Gal A in Fabry Lymphoblasts.

Structural Basis of in vitro Inhibition of α-Gal A

The summary of IC₅₀ and selected K_(i) values of DGJ and its derivatives are shown in Table 2.

TABLE 2 In vitro inhibition of α-Gal A by DGJ derivatives. IC₅₀ values (i.e. inhibitor concentration giving 50% inhibition) were determined by variation of inhibitor concentrations. K_(i) values were evaluated from the slope of Lineweaver-Burk plots. Assays were performed as described under “Methods.” All constants are expressed in micromolar. Inhibitor IC₅₀ and (K_(i))^(a) 1-deoxynojirimycin (DNJ) (1) 830 manno-DNJ (2) N.I.^(b) allo-DNJ (3) N.I. galacto-DNJ (DGJ) (4) 0.04 (K_(i), 0.04) gulo-DNJ (5) N.I. 2-deoxy-DGJ (6) 250 α-homonojirimycin (α-HNJ) (7) N.I. α-manno-HNJ (8) 464 α-allo-HNJ (9)  4.3 (K_(i), 2.6) α-galacto-HNJ (α-HGJ) (10) 0.21 (K_(i), 0.17) N-methyl-DGJ (11)  96 N-ethyl-DGJ (12) 306 N-propyl-DGJ (13) 301 N-butyl-DGJ (14) 300 N-hydroxyethyl-DGJ (15) 520 β-1-C-butyl-DGJ (16)   24 (K_(i), 16) ^(a)Km of α-Gal A was determined as 0.17 mM with p-nitrophenyl-α-D-galactopyranoside. ^(b)Inhibition was less than 50% at 1000 μM. DGJ and its Isomers

DGJ (galacto-DNJ) was synthesized from D-glucose and found to be an extremely powerful inhibitor of coffee bean α-galactosidase (39). In the development of the present invention, both IC₅₀ and K_(i) values of DGJ toward human lysosomal α-Gal A were calculated to be 0.04 μM (Table 2, FIG. 3A). DNJ (1) was a weak inhibitor of this enzyme with an IC₅₀ value of 830 μM, while other isomers such as manno- (2), allo- (3), and gulo-DNJ (5) showed no appreciable inhibition even at 1000 μM. The deoxygenation at C-2 of DGJ (6) reduced its inhibitory potential over 6000-fold. These results suggested to Applicants that a galactosyl configuration of an imino sugar is preferable for the inhibition of α-Gal A.

α-HNJ and Isomers

α-HNJ (7) was not an inhibitor of α-Gal A, but α-manno-HNJ (8) was a weak inhibitor of the enzyme. α-galacto-HNJ (10) mimicking α-D-galactopyranose was first expected to be a more specific and potent inhibitor of α-Gal A than DGJ. From ¹H-NMR studies, the ³J_(H,H)-coupling constants (J_(2,3)=9.8 Hz, J_(3,4)=3.0 Hz, J_(4,5)=2.6 Hz,) observed for α-galacto-HNJ (10) clearly showed that this compound is predominantly in a chair conformation which maintained the ground-state structure of the substrate. However, insertion of a hydroxymethyl group to the α-anomeric position of DGJ decreased the affinity for α-Gal A by approximately 4-fold. Surprisingly, α-allo-HNJ (9) showed a fairly potent inhibitory activity toward α-Gal A, with an IC₅₀ value of 4.3 μM. From its structure, this compound could form two different conformations as shown in FIG. 2, α-allo-HNJ (FIG. 2A) vs. C-2 epimer of α-galacto-HNJ (FIG. 2B). The J_(H,H) coupling constants in compound 9 (J_(1,2)=4.6 Hz; J_(2,3)=2.9 Hz; J_(3,4)=2.9 Hz; J_(4,5=6.5) Hz) indicated that the conformation deviates from a chair form as a result of the 1,3 syn-diaxial interaction between the substituents at C-2 and C-4 (FIG. 2B). Furthermore, the C-5 carbon in the ¹³C-NMR spectrum of 9 is observed as a broad signal, presumably due to “wobble” at C-5. The potent inhibitory activity of α-allo-HNJ (9) toward α-Gal A may be due to the partial stereochemical and conformational similarities between a flexible α-allo-HNJ conformation (FIG. 2C) and a galactosyl cation (FIG. 2D), which has been presumed to be a transition state intermediate in the enzyme-catalyzed galactoside hydrolysis (40).

N-Alkyl Derivatives of DGJ

The N-alkyl derivatives of DGJ were studied for α-Gal A inhibition because N-alkylation of DNJ and α-HNJ resulted in analogues with increased potency and substrate specificity on digestive α-glucosidases and processing α-glucosidase I (41–44), and N-alkylation of DNJ and DGJ increased inhibitory potential toward glucosyltransferase (45, 46). However, N-alkylation of DGJ markedly lowered its inhibitory activity toward α-Gal A (Table 3), suggesting that modification of the imino group is not preferred for inhibition of α-Gal A. The naturally occurring DGJ derivative, β-1-C-butyl-DGJ, has recently been isolated from Adenophorae Radix as a potent inhibitor of coffee bean α-galactosidase with an IC₅₀ value of 0.71 μM (35). The IC₅₀ value for α-Gal A was determined to be 24 μM.

Inhibition Mode of DGJ and its Derivatives

The inhibition mode of four potent inhibitors of α-Gal A, DGJ (4), α-galacto-HNJ (10), α-allo-HNJ (9) and β-1-C-butyl-DGJ (16) were studied. Lineweaver-Burk plots indicated that they are competitive inhibitors of α-Gal A (FIG. 3). The calculated Ki values of DGJ, α-galacto-HNJ, α-allo-HNJ and β-1-C-butyl-DGJ were found to be 0.04 μM, 0.25 μM, 2.6 μM, and 16 μM, respectively.

Intracellular Enhancement of α-Gal A by the Enzyme Inhibitors

As shown in FIG. 4B, those DGJ derivatives that showed high inhibitory activity toward α-Gal A were tested for enhancement of intracellular α-Gal A activity in R301Q lymphoblasts. Treatment with DGJ at 100 μM for 4 days increased enzyme activity in R301Q lymphoblasts by about 14-fold reaching 49% of normal. Enzyme activity was increased 5.2-fold, 2.4-fold, and 2.3-fold by cultivation with α-galacto-HNJ, α-allo-HNJ and β-1-C-butyl-DGJ at 100 μM, respectively, while weak inhibitors such as N-alkyl derivatives of DGJ showed only a slight enhancement effect at 100 μM. The effectiveness of intracellular enhancement paralleled to the in vitro inhibitory activity (FIG. 4A), indicating that a potent inhibitor serves as an effective enhancer.

The enzyme activity in R301Q lymphoblasts was elevated with increasing inhibitor concentration in a certain range (for DGJ, 1–100 μM, FIG. 5). α-galacto-HNJ, α-allo-HNJ, and β-1-C-butyl-DGJ enhanced the α-Gal A activity by 12.5-, 3.9-, and 6.3-fold at 1000 μM, respectively. However, higher concentrations significantly reduced the enhancement effect, presumably causing inhibition of the enzyme activity. Applicants confirmed that inclusion of DGJ in the medium at 20 μM did not cause intracellular inhibition of globotriaosylceramide metabolism, indicating that intracellular DGJ concentration appeared to be lower than the concentration normally required to inhibit the intracellular enzyme activity at that condition (24). Intralysosomal enzyme activity may not be inhibited by α-galacto-HNJ, α-allo-HNJ, and β-1-C-butyl-DGJ added in the culture medium at 1000 μM, because these compounds exhibited weaker inhibitory activity than DGJ.

Although β-1-C-butyl-DGJ was a less effective inhibitor of α-Gal A than α-allo-HNJ (K_(i)=16 μM vs K_(i)=2.6 μM), both enhancement effects were the same at 100 μM, and the effect of β-1-C-butyl-DGJ at 1000 μM was higher than that by α-allo-HNJ at the same concentration (FIG. 5). This suggested that the bioavailability of β-1-C-butyl-DGJ may be better than α-allo-HNJ, because increase of lipophilicity resulting from the C-alkylation at C-1 of DGJ may enhance the efficient transport across cell and ER membranes.

Calystegine compounds are polyhydroxylated nortropane alkaloids. Certain of these alkaloids exhibit potent inhibitory activities against glycosidases (47). The enzyme activity in R301Q lymphoblasts was also elevated with increasing concentration of calystegine A₃ (FIG. 6A), calystegine B₂ (FIG. 6B), N-methyl-calystegine A₃ (FIG. 6C), and N-methyl-calystegine B₂ (FIG. 6D), respectively in a range of 100–1000 μM.

The above results further supported Applicants' therapeutic concept that potent competitive inhibitors can serve as efficient chemical chaperones to enhance intracellular mutant enzyme activity in cells derived from patients of Fabry disease. According to this theoretical concept, more potent inhibitors serve as more powerful chemical chaperones. As shown in the following examples, this therapeutic strategy of using potent competitive inhibitors or substrate analogs is not limited to Fabry disease, but also applicable to other lysosomal storage disorders and general hereditary disorders resulted from protein folding defects, such as, but not limited to, α₁-antitrypsin deficiency, familial hypercholesterolemia, Alzheimer's disease, Marfan syndrome, osteogenesis imperfecta, carbohydrate-deficient glycoprotein syndrome, and Maroteaux-Lamy syndrome.

EXAMPLE 2

Intracellular Enhancement of β-Galactosidase Activity in Fibroblasts from G_(M1)-Gangliosidosis Patients.

G_(M1)-gangliosidosis is a progressive neurological disease caused by hereditary deficiency of lysosomal acid β-galactosidase (β-Gal) which hydrolyses the terminal β-galactosidic residual of ganglioside G_(M1) and other glycoconjugates (27). Three clinical forms are described as infantile type severe form), juvenile type (sub-severe type), and adult onset type (mild type). No treatment is available for this disorder.

Applicants applied the strategy of using potent inhibitors as chemical chaperones to enhance intracellular mutant enzyme activity to human G_(M1)-gangliosidosis fibroblasts. Human G_(M1)-gangliosidosis fibroblasts were cultured for 5 days with DGJ (4) and 4-epi-isofagomine (21) (both are inhibitors of β-Gal) at 500 μM, and 50 μM, respectively (FIG. 6). The enhancement effect was not efficient with the fibroblasts from patients of infant type disease (BGF-1 and BGF-6). However, the intracellular enzyme activities in fibroblasts established from patients diagnosed as juvenile and adult types disease were elevated to 9–53% of normal (FIG. 7B). The residual enzyme activity in BGF-7 was markedly increased 27-fold by inclusion of compound 4 at 500 μM (FIG. 7A). These results indicate that compound 4 and 21 are powerful chemical chaperones for β-Gal, and can be used as potential therapeutic agents for treatment of G_(M1)-gangliosidosis.

EXAMPLE 3

Intracellular Enhancement of Glucocerebrosidase Activity in Fibroblasts from Gaucher Patients.

Gaucher disease is characterized by the accumulation of glucosylceramide (glucocerebroside) due to the deficient activity of lysosomal acid β-glucosidase (glucocerebrosidase, β-Glu) (26). Three types of Gaucher disease have been identified: 1) type 1 (adult-onset), lack of primary central nervous system involvement; 2) type 2 (infantile-onset), acute neuronopathic form of the disease with an early onset; type 3 (late-infantile/juvenile-onset), subacute neuronopathic form. Enzyme replacement therapy is effective only for type 1 disease.

In Vitro Inhibition of Glucocerebrosidase

Various natural and synthetic compounds were tested with human normal β-Glu for inhibitory activity, and the IC₅₀ values are shown in Table 3.

TABLE 3 In vitro inhibition of human β-glucocerebrosidase. IC₅₀ values were determined by variation of inhibitor concentrations. Assays were performed with glucocerebrosidase in 0.1 M citrate buffer (pH 5.2) using 4-MU-β-Glu as substrate. All constants are expressed in micromolar. Inhibitor IC₅₀ Calystegine A₃ (17) 3.1 Calystegine A₅ (22) 31 Calystegine B₁ (23) 2.5 Calystegine B₂ (18) 0.99 Calystegine B₃ (24) 76 Calystegine B₄ (25) 82 Calystegine C₁ (26) 2.5 N-Metyl-calystegine B₂ (20) 320 DMDP (27) 280 DAB (28) 160 Castanospermine (29) 19 DNJ (1) 240 N-Butyl-DNJ (30) 270 N-Dodecyl-DNJ (31) 0.05 DNJ bisulfite (32) 28 Isofagomine (33) 0.04 N-Butyl-isofagomine (34) 44 N-(3-cyclohexylpropyl)-isofagomine (35) 100 N-(3-phenylpropyl)-isofagomine (36) 69 N-[(2E,6Z,10Z)-3,7,11- 1.5 trimethyldodecatrienyl]-isofagomine (37)

Several potent inhibitors were found among calystegine compounds. Calystegine B₂ (18) (IC₅₀ value, 0.99 μM), calystegine B₁ (23) (2.5 μM), calystegine Ca (26) (2.5 μM), and calystegine A₃ (17) (3.1 μM) were the best inhibitors in this class. Castanospermine (29) is a known potent inhibitor for α-glucosidase, however, it also present fair inhibitory activity against β-Glu (19 μM). DNJ (1) and N-butyl-DNJ (30) were weak inhibitors for this enzyme, however, N-dodecyl-DNJ (31) turned to be one of the most potent inhibitor with IC₅₀ at 0.05 μM. Since DNJ and N-butyl-DNJ were moderate inhibitors of the enzyme, the high potency of this compound (31) is believed from the long alkyl chain in the molecular which is probably recognized by the recognition domain normally recognizing the ceramide part of the substrate. Isofagomine (IFG, 33) was reported as a potent inhibitor against almond β-galactosidase (40), and revealed as the most potent inhibitor among those tested with IC₅₀ value at 0.04 μM. Modification of the imino group (compounds 34–37) of IFG reduced inhibitory activity substantially. This result consistent with Applicants' earlier finding with α-Gal A in which alkyl modification of DGJ nullified its inhibitory activity. Noticeably, compound 37 which contains a 12 carbon chain in the backbone increased 30-fold in its potency compared with compound 32 which contains a 4 carbon chain. Combined with the result generated from DNJ (1) and N-dodecyl-DNJ (31), it is expected that N-dodecyl-IFG serves as a powerful inhibitor for human β-Glu. In accordance with the invention, these inhibitors should be effective in enhancing activity of the defective enzyme associated with Gaucher disease and treatment of the disorder.

Intracellular Enhancement of β-Glu Activity in Fibroblasts from Gaucher Patients

Isofagomine and derivatives IFG (33) is the most potent inhibitor tested for β-Glu in vitro. Its intracellular enhancement activity was investigated with fibroblasts established from a Gaucher patient with N370S/N370S genotype. The intracellular enzyme activity was increased 55–80% by cultivation the cell with IFG added in the culture medium at 1–50 μM (FIG. 8A). Higher than 50 μM concentration nullified the enhancement effect. The enhancement effect was monitored for 5 days. The residual enzyme activity in Gaucher cells did not change on day 1 or 2, however, the enzyme activity was elevated alter day 3 and increased more than 80% at day 5 (FIG. 8B). This data demonstrated that IFG, a potent inhibitor of β-Glu, also serves as an enhancer for residual β-Glu in the cells derived from Gaucher patients when a appropriate concentration is applied. Effective concentrations are expected to be lower than those needed to inhibit the enzyme, but will be able to be determined through routine experimentation by those of skill in the art for Gaucher disease and other disorders. IFG derivatives (compounds 34–37) demonstrated significant impact on enhancement of the intracellular enzyme activity in Gaucher cells (N370S/N370S) cultivated with these compounds (FIG. 9). The residual enzyme activity was elevated 73% (compound concentration at 10 μM) and 56% (100 μM) by compound 34, 106% (10 μM) and 47% (100 μM) by compound 35, and 50% (10 μM) and 54% (100 μM) by compound 36, respectively. The residual enzyme activity was increased 43% by cultivation with compound 37 at 10 μM, however, decreased 53% with the compound at 100 μM. Although the inhibitory activity of the IFG derivatives was weaker than IFG, the intracellular enhancement activity of the IFG derivatives appears to be higher than IFG, since they achieved higher elevation of the mutant enzyme activity at lower concentrations. It is believed that the bioavailability of these compounds is significantly improved by the hydrophobic nature of the molecule, leading to easier crossing of cell and the ER membranes, thereby increasing the intracellular concentration of these compounds. Particularly, compound 37 at 100 μM decreased the residual activity, presumably intracellular concentration reached to the concentration required for inhibition.

N-dodecyl-DNJ N-dodecyl-DNJ (31) is one of the most potent inhibitors of β-Glu tested, and is believed to be recognized by the domain usually recognizing ceramide of the natural substrate. N-dodecyl-DNJ also enhanced β-Glu activity in fibroblasts derived from Gaucher patient with N370S/N370S mutation. The enzyme activity increased 95% by cultivation the cells with N-dodecyl-DNJ at 0.5 μM for 5 days (FIG. 10A). The elevation of enzyme activity was dose-dependent between the concentrations of 0.05–0.5 μM added to the medium. However, N-dodecyl-DNJ at higher than 1 μM nullified the enhancement effect. The time course of cultivation of the cells with N-dodecyl-DNJ at 0.5 μM indicated that the residual enzyme activity increased after day 3 (FIG. 10B). Since N-dodecyl-DNJ and IFG are recognized by different recognition domains of the enzyme (N-dodecyl-DNJ, ceramide recognition domain vs. IFG, glucoside recognition domain), a compound with a combination of N-dodecyl-DNJ and IFG such as N-dodecyl-IFG is expected to be a powerful agent for enhancing residual enzyme activity in Gaucher cells.

Calystegine compounds Calystegine A₃ (17), calystegine B₁ (23), calystegine B₂ (18) and calystegine C₁ (26) exhibited potent inhibitory activity against β-Glu and were tested for intracellular enhancement of β-Glu activity with fibroblasts derived from Gaucher patient with a genotype of L444P/L444P (FIG. 11). The residual enzyme activity in the patient's cells was increased 230%, 76%, 126% and 136% by cultivation with calystegine B₂, B₁, A₃ and C₁ at 10 μM, respectively. The results indicate that these compounds also act as effective enhancers for Gaucher fibroblasts.

Applicants have shown that i) α-allo-HNJ (9), α-HGJ (10), β-1-C-butyl-DGJ (16), calystegine A₃ (17), calystegine B₂ (18), N-metyl calystegine A₃ (19), and N-methyl calystegine B₂ (20) are able to effectively increase the intracellular α-Gal A activity in Fabry lymphoblasts by cultivation the cells with the above individual compound in concentration ranges of 10–1000 μM; ii) DGJ (4) and 4-epi-isofagomine (21) are able to effectively enhance the intracellular β-Gal activity in G_(M1)-gangliosidosis fibroblasts by cultivation the cells with the above individual compound in concentration ranges of 50–500 μM; iii) Calystegine B₂ (18), calystegine B₁ (23), calystegine A₃ (17), calystegine C₁ (26), N-dodecyl-DNJ (31), isofagomine (33), N-butyl-isofagomine (34), N-(3-cyclohexylpropyl)-isofagomine (35), N-(3-phenylpropyl)-isofagomine (36) and N-[(2E,6Z,10Z)-3,7, 1-trimethyldodecatrienyl]-isofagomine (37) are able to effectively enhance the intracellular β-Glu activity in Gaucher fibroblasts by cultivation the cells with the above individual compound in concentration ranges of 0.05–100 μM.

Applicants earlier disclosed in U.S. application Ser. No. 09/087,804 a method for treatment of Fabry disease by administration of potent competitive inhibitors of α-Gal A to enhance the intracellular α-Gal A activity in the Fabry lymphoblsts. The mechanism underlying this treatment is believed to be that the competitive inhibitors serve as chemical chaperones to induce/ensure the proper (native) conformation of the mutant protein for a smooth escape from the ER quality control system, thus accelerate the maturation and transport leading to increase of the intracellular enzyme activity. In the present application, Applicants further demonstrate the correlation between in vitro inhibition and intracellular enhancement with a series of inhibitors for α-Gal A. The results clearly show that more potent competitive inhibitors serve as more powerful enhancers for the mutant enzyme.

In the present application, it is demonstrated that the method for treatment of Fabry disease by administration of potent competitive inhibitor of the defective enzyme can be applied to G_(M1)-gangliosidosis and Gaucher disease, both diseases belong to lysosomal storage disorder family, and potent inhibitors for β-Gal or β-Glu can effectively enhance the intracellular enzyme activities in the fibroblasts established from patients of G_(M1)-gangliosidosis or Gaucher disease, respectively. Since the lysosomal storage disorders share the same biological and biochemical pathogenic mechanisms, this method of using potent competitive inhibitors of the defective enzyme is expected to be applicable for the treatment of other lysosomal storage disorders listed in Table 1.

Recent study on glycosidase inhibitors showed that conventional type of iminosugars having a nitrogen atom replacing the ring oxygen of a sugar such as 1-deoxynojirimycin are more potent and selective inhibitors for α-glycosidases, whereas 1-N-iminosugars having a nitrogen atom at the anomeric position of the pyranose ring are more potent and selective for β-glycosidases (40). We expect that conventional type of iminosugars (nojirimycin type), e.g., 1-deoxy-nojirimycin, 1-deoxy-galactonojirimycin, 1-deoxy-iduronojirimycin, 1,2-dideoxy-2-N-acetamido-nojirimycin, 1-deoxymannonojirimycin, 1-deoxyfuconojirimycin, 2,6-dideoxy-2,6-imino-sialic acid, and 1,2-dideoxy-2-N-acetamido-galactonojirimycin (FIG. 12), which have it ground-state structure of the substrate of a defective enzyme, e.g., α-glucosidase, α-galactosidase, α-L-iduronidase, α-N-acefylglucosamimidase, α-mannosidase, α-L-fucosidase, α-N-acetyl-neuramimidase, and α-N-acetylgalactosamimidase, are potent inhibitors and powerful enhancers for treatment of Pompe disease, Fabry disease, Hurler-Scheie disease, Sanfilippo disease, α-mannosidosis, Fucosidosis, Sialidosis and Schindler-Kanzaki disease, respectively. We also expect that 1-N-iminosugars, e.g., isofagomine, 4-epi-isofagomine, 2-N-acetamido-isofagomine, 6-carboxy-isofagomine, and 2-hydroxy-isofagomine (FIG. 12), which have a ground-state structure of the substrate of a defective enzyme, e.g., β-glucosidase, β-galactosidase, β-N-acetylglucosamimidase, β-glucuronidase, and β-mannosidase, are potent inhibitors and powerful enhancers for treatment of Gaucher disease, G_(M1)-gangliosidosis, Krabbe disease, Morquio disease, Tay-Sachs disease, Sandohoff disease, Sly disease, and β-mannosidosis. A summary of potent competitive inhibitors which are expected to effectively enhance the mutant enzyme activity associated with lysosomal storage disorders is presented in Table 4.

TABLE 4 Summary of expected enhancers for lysosomal storage disorders. Disorder Targeting enzyme Enhancer Ref. Pompe disease α-glucosidase 1-deoxynojirimycin (DNJ) 28 α-homonojirimycin 31 castanospermine *11 Gaucher disease Acid β-glucosidase, or isofagomine 40 glucocerebrosidase N-dodecyl-DNJ *1 calystegines A₃, B₁, B₂, C₁ *1 Fabry disease α-galactosidase A 1-deoxygalactonojirimycin 24 α-allo-homonojirimycin *2 α-galacto-homonojirimycin *2 β-1-C-butyl-deoxynojirimycin *2 calystegines A₃, B₂ *1 N-methyl calystegines A₃, B₂ *1 G_(M1)-gangliosidosis Acid β-galactosidase 4-epi-isofagomine *1 1-deoxygalactonojirimycin *1 Krabbe disease Galactocerebrosidase 4-epi-isofagomine 40 1-deoxygalactonojirimycin 28 Morquio disease B Acid β-galactosidase 4-epi-isofagomine 40 1-deoxygalactonojirimycin 28 α-Mannosidosis Acid α-mannosidase 1-deoxymannojirimycin 40 Swainsonine *3 Mannostatin A *4 β-Mannosidosis Acid β-mannosidase 2-hydroxy-isofagomine 40 Fucosidosis Acid α-L-fucosidase 1-deoxyfuconojirimycin *5 β-homofuconojirimycin *5 2,5-imino-1,2,5-trideoxy-L-glucitol *5 2,5-dideoxy-2,5-imino-D-fucitol *5 2,5-imino-1,2,5-trideoxy-D-altritol *5 Sanfilippo disease B α-N-Acetylglucosaminidase 1,2-dideoxy-2-N-acetamido-nojirimycin 40 Schindler-Kanzaki α-N- 1,2-dideoxy-2-N-acetamido- 40 disease acetylgalactosaminidase galactonojirimycin Tay-Sachs disease β-Hexosaminidase A 2-N-acetylamino-isofagomine 40 1,2-dideoxy-2-acetamido-nojirimycin *6 nagstain and its derivatives *7, *8 Sandhoff disease β-Hexosaminidase B 2-N-acetamido-isofagomine 40 1,2-dideoxy-2-acetamido-nojirimycin *6 nagstain and its derivatives *7, *8 Hurler-Scheie disease α-L-Iduronidase 1-deoxyiduronojirimycin 40 2-carboxy-3,4,5-trideoxypiperidine *9 Sly disease β-Glucuronidase 6-carboxy-isofagomine 40 2-carboxy-3,4,5-trideoxypiperidine *9 Sialidosis Sialidase 2,6-dideoxy-2,6-imino-sialic acid 40 Siastatin B *10 References: *1, This application. *2, Asano, N., Ishii, S., Kizu, H., Ikeda, K., Yasuda, K., Kato, A., Martin, O. R., and Fan, J. -Q. (2000) In vitro inhibition and intracellular enhancement of lysosomal α-galactosidase A activity in Fabry lymphoblasts by 1-deoxygalactonojirimycin and its derivatives. Eur. J. Biochem., in press. *3, Dorling, P. R., Huxtable, C. R., and Colegate, S. M. (1980) Inhibition of lysosomal α-mannosidase by swainsonine isolated from Swainsona canescens. Biochem. J. 191, 649–651. *4, Aoyagi, T., Yamamoto, T., Kojiri, K., Morishima, H., Nagai, M., Hamada, M., Takeuchi, T., and Umezawa, H., (1989) Mannostatins A and B: new inhibitors of alpha-D-mannosidase, produced by Streptoverticillium verticillus var. quintum ME3-AG3: taxonomy, production, isolation, physico-chemical properties and biological activities. J. Antibiot. 42, 883–889. *5, Asano, N., Yasuda, K., Kizu, H., Kato, A., Fan, J. -Q., Nash, R. J., Fleet, G. W. J., and Molyneux, R. J. (2000) Novel α-L-fucosidase inhibitors from the bark of Angylocalyx pynaertii (Leguminosae). Submitted. *6, Fleet, G. W. J., Smith, P. W., Nash, R. J., Fellows, L. E., Parekh, R. J., and Rademacher, T. W. (1986) Synthesis of 2-acetamido-1,5-imino-1,2,5-trideoxy-D-mannitol and of 2-acetamido-1,5-imino-1,2,5-trideoxy-D-glucitol, a potent and specific inhibitor of a number of β-N-acetylglucosaminidases. Chem. Lett. 1051–1054. *7, Aoyagi T, Suda H, Uotani K, Kojima F, Aoyama T, Horiguchi K, Hamada M, Takeuchi T (1992) Nagstatin, a new inhibitor of N-acetyl-beta-D-glucosaminidase, produced by Streptomyces amakusaensis MG846-fF3. Taxonomy, production, isolation, physico-chemical properties and biological activities. J Antibiot (Tokyo) 45, 1404–8. *8, Tatsuta K, Miura S, Ohta S, Gunji H (1995) Syntheses and glycosidase inhibiting activities of nagstatin analogs. J Antibiot (Tokyo) 48, 286–8. *9, Cenci di Bello I, Dorling P, Fellows L, Winchester B (1984) Specific inhibition of human β-D-glucuronidase and α-L-iduronidase by a trihydroxy pipecolic acid of plant origin. FEBS Lett 176, 61–4. *10, Umezawa H, Aoyagi T, Komiyama T, Morishima H, Hamada M (1974) Purification and characterization of a sialidase inhibitor, siastatin, produced by Streptomyces. J Antibiot (Tokyo) 27, 963–9. *11, Pili R, Chang J, Partis RA, Mueller RA, Chrest FJ, Passaniti A (1995) The alpha-glucosidase I inhibitor castanospermine alters endothelial cell glycosylation, prevents angiogenesis, and inhibits tumor growth. Cancer Res 55, 2920–6.

References cited herein are hereby incorporated by reference and are listed below for convenience.

-   1. Anfinsen, C. B., Scheraga, H. A. (1975) Experimental and     theoretical aspects of protein folding. Adv. Protein Chem. 29,     205–300. -   2. Hartl, F. U. (1996) Molecular chaperones in cellular protein     folding. Nature 381, 571–580. -   3. Gething, M. J., Sambrook, J. (1992) Protein folding in the cell.     Nature 355, 33–45. -   4. Caplan, A. J. (1999) Hsp90's secrets unfold: New insights from     structural and functional studies. Trends Cell Biol. 9, 262–268. -   5. Lin, H., Masso-Welch, P., Di, Y. Cai, J. W., Shen, J. W. and     Subjeck, J. R. (1993) The 170-kDa glucose-regulated stress protein     is an endoplasmic reticulum protein that binds immunoglobulin. Mol.     Biol. Cell 4, 1109–1119. -   6. Bergeron, J. J. M., Brenner, M. B., Thomas, D. Y. and     Williams, D. B. (1994) Calnexin: A membrane-bound chaperone of the     endoplasmic reticulum. Trends Biochem. Sci. 19, 124–128. -   7. Haas, I. G. (1991) Bip—a heat shock potein involved in     immunoglobulin chain assembly. Curr. Top Microbiol. Immunol. 167,     71–82. -   8. Hurtley, S. M., and Helenius, A. (1989) Protein oligomerization     in the endoplasmic reticulum. Annu. Rev. Cell Biol. 5, 277–307. -   9. Kuznetsov, G., and Nigam, S. K. (1998) Folding of secretory and     membrane proteins. N. Engl. J. Med. 339, 1688–1695. -   10. Thomas, P. J., Qu, B. H., and Pedersen, P. L. (1995) Defective     protein folding as a basis of human disease. Trends Biochem. Sci.     20, 456–459. -   11. Bychkova, V. E., and Ptitsyn, O. B. (1995) Folding intermediates     are involved in genetic diseases? FEBS Lett. 359, 6–8. -   12. Brooks, D. A. (1997) Protein processing: a role in the     pathophysiology of genetics disease. FEBS Lett. 409, 115–120. -   13. Yang, Y., Janich, S., Cohn, J. A., and Wilson, J. M. (1993) The     common variant of cystic fibrosis transmembrane conductance     regulator is recognized by hsp70 and degraded in a pre-Golgi     nonlysosomiial compartment. Proc. Natl. Acad. Sci. USA 90,     9480–9484. -   14. Ward, C. L., Omura, S., and Kopito, R. R. (1995) Degradation of     CFTR by the ubiquitin-proteasome pathway. Cell 83, 121–127. -   15. Pasyk, E. A., and Foskett, J. K. (1995) Mutant (ΔF508) cystic     fibrosis transmembrane conductance regulator Cl⁻ channel is     functional when retained in endoplasmic reticulum of mammalian     cells. J. Biol. Chem. 270, 12347–12350. -   16. Lomas D. A., Evans, D. L., Finch, J. T., and     Carrell, R. W. (1992) The mechanism of Z α₁-antitrypsin accumulation     in the liver. Nature 357, 605–607. -   17. Qu, D., Teckman, J. H., Omura, S., and Perlmutter, D. H. (1996)     Degradation of a mutant secretory protein, α₁-antitrypsin Z, in the     endoplasmic reticulum requires proteasome activity. J. Biol. Chem.     271, 22791–22795. -   18. Djordjevic, J. T., Bieri, S., Smith, R., and Kroon, P. A. (1996)     A deletion in the first cysteine-rich repeat of the     low-density-lipoprotein receptor leads to the formation of multiple     misfolded isomers. Eur. J. Biochem. 239, 214–219. -   18a. Selkoe, D. J. (1994) Normal and abnormal biology of the     β-amyloid precursor protein. Ann. Rev. Neurosci. 17, 489–517. -   19. Ramirez, F. (1996) Fibrillln mutations in Marfan syndrome and     related phenotypes. Curr. Opin. Genet. Dev. 6, 309–315. -   20. Chessler, S. D., and Byers, P. H. (1993) BiP binds type I     procollagen pro alpha chains with mutations in the carboxyl-terminal     propeptide synthesized by cells from patients with osteogenesis     imperfecta. J. Biol. Chem. 268, 18226–18233. -   21. Marquardt, T., Ullrich, K., Zimmer, P., Hasilik, A., Deufel, T.,     and Harms, E. (1995) Carbohydrate-deficient glycoprotein syndrome     (CDGS)—glycosylation, folding and intracellular transport of newly     synthesized glycoproteins. Eur. J. Cell. Biol. 66, 268–273. -   22. Bradford, T. M., Gething, M. J., Davey, R., Hopwood, J. J., and     Brooks, D. A. (1999) Processing of normal lysosomal and mutant     N-acetylgalactosamine 4-sulphatase: BiP (immunoglobulin heavy-chain     binding protein) may interact with critical protein contact sites.     Biochem. J. 341, 193–201. -   23. Desnick, R. J., loannou, Y. A. and Eng, C. M. ∀-Galactosidase A     deficiency: Fabry disease. in The Metabolic and Molecular Bases of     Inherited Disease (eds. Scriver, C. R., Beaudet, A. L., Sly, W. S.     and Valle, D.), 2741–2784 (McGraw-Hill, New York, 1995). -   24. Fan, J.-Q., Ishii, S., Asano, N. and Suzuki, Y. (1999)     Accelerated transport and maturation of lysosomal α-galactosidase A     in Fabry lymphoblasts by an enzyme inhibitor. Nature Med. 5,     112–115. -   25. Ishii, S., Kase, R., Sakuraba, H., and Suzuki, Y. (1993)     Characterization of a mutant α-galactosidase gene product for the     late-onset cardiac form of Fabry disease, Biochem. Biophys. Res.     Comm. 197, 1585–1589. -   25a. Leinekugel, P., Michel, S., Conzelmann, E., and     Sandhoff, K. (1992) Quantitative correlation between the residual     activity of beta-hexosammidase A and arylsulfatase A and the     severity of the resulting lysosomal storage disease. Hum. Genet. 88,     513–23. -   25b. Kappler, J., Watts, R. W., Conzelmann, E., Gibbs, D. A.,     Propping, P., and Gieselmann, V. (1991) Low arylsulphatase A     activity and choreoathetotic syndrome in three siblings:     Differentiation of pseudodeficiency from metachromatic     leukodystrophy. Eur. J. Pediatr. 150, 287–290. -   26. Beutler, E., and Grabowski, G. A. Gaucher disease. in The     Metabolic and Molecular Bases of Inherited Disease (eds. Scriver, C.     R., Beaudet, A. L., Sly, W. S. and Valle, D.), 2641–2670     (McGraw-Hill, New York, 1995). -   27. Suzuki, Y., Sakuraba, H., and Oshima, A. β-Galactosidase     deficiency (β-galactosidosis): G_(M1)-gangliosidosis and Morquio B     disease. in The Metabolic and Molecular Bases of Inherited Disease     (eds. Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D.),     2785–2824 (McGraw-Hill, New York, 1995). -   28. Asano, N., Oseki, K., Tomioka, E., Kizu, H., and     Matsui. K. (1994) N-containing sugars from Morus alba and their     glycosidase inhibitory activities. Carbohydr. Res. 259, 243–255. -   29. Asano, N., Oseki, K., Kizu, H., and Matsui, K. (1994)     Niltrogen-in-the-ring pyranoses and furanoses: structural basis of     inhibition of mammalian glycosidases. J. Med. Chem. 37, 3701–3706. -   30. Heiker, F.-R. and Schueller, A. M. (1990) Synthesis of     D-galacto-1-deoxynojirimycin (1,5-dideoxy-1,5-imino-D-galactitol)     starting from 1-deoxynojirimycin. Carbohydr. Res. 203, 314–318. -   31. Asano, N., Nishida, M., Kizu, H., and Matsui, K. (1997)     Homonojirimycin isomers and glycosides from Aglaonema treubii J.     Nat. Prod. 60, 98–101. -   32. Martin, O. R., Compain, P., Kizu, H., and Asano, N. (1999)     Revised structure of a homonojirimycin isomer from Aglaonema     treubii: first example of a naturally occurring     α-homoallonojirimycin. Bioorg. Med. Chem. Lett. 9, 3171–3174. -   33. Martin, O. R., Xie, F., and Liu, L. (1995) Synthesis of     “α-homogalactostatin” and of its 1,N-anhydro derivative. Tetrahedron     Lett. 36, 4027–4030. -   34. Kato, H., Koshinaka, E., Arata, Y., and Hanaoka, M. (1973)     Studies on 1-azabicyclo compound. XVI. Synthesis of     1′-methylindan-2-spiro-2′-piperazine and related compounds. Chem.     Pharm. Bull. 21, 2661–2666. -   35. Ikeda, K., Takahashi, M., Nishida, M., Miyauchi, M., Kizu, H.,     Kameda, Y., Arisawa, M., Watson, A. A., Nash, R. J., Fleet, G. W.     J., and Asano, N. (1999) Carbohydr. Res., 323, 73–80. -   36. Asano N, Kato A, Matsui K, Watson A A, Nash R J, Molyneux R J,     Hackett L, Topping J, Winchester B (1997) The effects of     calystegines isolated from edible fruits and vegetables on mammalian     liver glycosidases. Glycobiology 7, 1085–8. -   37. Ishii, S., Kase, R., Sakuraba, H., Fujita, S., Sugimoto, M.,     Tomita, K., Semba, T., and Suzuki, Y. (1994) Human α-galactosidase     gene expression: significance of two peptide regions encoded by     exons 1–2 and 6. Biochem. Biophys. Acta 1204, 265–270. -   38. Ishii, S., Kase, R., Sakuraba, H., and Suzuki, Y. (1993)     Characterization of a mutant α-galactosidase gene product for the     late-onset cardiac form of Fabry disease. Biochem. Biophys. Res.     Comm. 197, 1585–1589. -   39. Legler, G. and Pohl, S. (1986) Synthesis of     5-amino-5-deoxy-D-galactopyranose and     1,5-dideoxy-1,5-imino-D-galactitol, and their inhibition of α- and     β-D-galactosidases. Carbohydr. Res. 155, 119–129. -   40. Ichiwaka, Y., Igarashi, Y., Ichikawa, M, and Suhara, Y. (1998)     1-N-Iminosugars: Potent and selective inhibitors of glycosidases. J.     Am. Chem. Soc. 120, 3007–3018. -   40a. Asano, N., Kato, A., Oseki, K., Kizu, H., and Matsui, K. (1995)     Calystegins of Physalis alkekengi var. francheti (Solanaceae).     Structure determination and their glycosidase inhibitory activities.     Eur. J. Biochem. 229, 369–76. -   41. Junge, B., Matzke, M., and Stoltefuss, J. (1996) Chemistry and     structure-activity relationships of glucosidase inhibitors. in     Handbook of Experimental Pharmacology (Born, G. V. R., Cuatrecasas,     P., Herken, H., and Melmon, K. L., eds) Vol. 119, pp. 411–482,     Springer-Verlag, Berlin Heiderberg. -   42. Schweden, J., Boegmann, C., Legler, G., and Bause, E. (1986)     Characterization of calf liver glucosidase I and its inhibition by     basic sugar analogs. Arch. Biochem. Biophys. 248, 335–340. -   43. Tan, A., van den Broek, L., van Boeckel, S., Ploegh, H., and     Bolscher, J. (1991) Chemical modification of the glucosidase     inhibitor 1-deoxynojirimycin. Structure-activity relationships J.     Biol. Chem. 266. 14504–14510. -   44. Zeng, Y., Pan, Y. T., Asano, N., Nash, R., and     Elbein, A. D. (1997) Homonojirimycin and N-methyl-homonojirimycin     inhibit N-linked oligosaccharide processing. Glycobiology 7,     297–304. -   45. Platt, F. M., Neises, G. R., Dwek, R. A., and     Butters, T. D. (1994) N-butyldeoxynojirimycin is a novel inhibitor     of glycolipid biosynthesis. J. Biol. Chem. 269, 8362–8365. -   46. Platt, F. M., Neises, G. R., Karlsson, G. B., Dwek, R. A., and     Butters, T. D. (1994) N-butyldeoxygalactonojirimycin inhibits     glycolipid biosynthesis but does not affect N-linked oligosaccharide     processing. J. Biol. Chem. 269, 27108–27114. -   47. Molyneux, R. J., Nash, R. J. and Asano, N. (1996) The chemistry     and biology activity of calystegines and related nortropane     alkaloids. In Alkaloids: chemical and biological Perspective, Vol 11     (Pelletier, S. W., ed.) pp 303–343. Elsevier Science, Oxford. 

1. A method for treating Gaucher disease, which method comprises administering to an individual in need thereof an amount of an isofagomine compound effective to enhance the activity of a mutant glucocerebrosidase enzyme.
 2. The method of claim 1, wherein the isofagomine compound is isofagomine.
 3. The method of claim 1, wherein the isofagomine compound is N-dodecyl-isofagomine.
 4. The method of claim 1, wherein the isofagomine compound is N-butyl-isofagomine.
 5. The method of claim 1, wherein the isofagomine compound is N-(3-cyclohexylpropyl)-isofagomine.
 6. The method of claim 1, wherein the isofagomine compound is N-(3-phenylpropyl)-isofagomine.
 7. The method of claim 1, wherein the isofagomine compound is N-[(2E,6Z,10Z)-3,7,11-trimethyldodecatrienyl]-isofagomine.
 8. The method of claim 1, wherein the mutant glucocerebrosidase results from a homozygous mutation in the glucocerebrosidase gene.
 9. The method of claim 1, wherein the mutant glucocerebrosidase enzyme mutation is N370S.
 10. The method of claim 1, wherein the Gaucher disease is type 1 Gaucher disease.
 11. The method of claim 2, wherein the glucocerebrosidase activity is enhanced by about 55–80% compared to activity of glucocerebrosidase in an individual not administered isofagomine.
 12. The method of claim 4, wherein the glucocerebrosidase activity is enhanced by about between 56–73% compared to activity of glucocerebrosidase in an individual not administered N-butyl-isofagomine.
 13. The method of claim 5, wherein the glucocerebrosidase activity is enhanced by about between 47–106% compared to activity of glucocerebrosidase in an individual not administered N-(3-cyclohexylpropyl)-isofagomine.
 14. The method of claim 6, wherein the glucocerebrosidase activity is enhanced by about between 50–54% compared to activity of glucocerebrosidase in an individual not administered N-(3-phenylpropyl)-isofagomine.
 15. The method of claim 7, wherein the glucocerebrosidase activity is enhanced by about 43% compared to activity of glucocerebrosidase in an individual not administered N-[(2E,6Z,IOZ)-3,7,11-trimethyldodecatrienyl]-isofagomine.
 16. A method for enhancing the activity of a lysosomal glucocerebrosidase enzyme in a mammalian cell, which comprises contacting the cell with an amount of an isofagomine compound effective to enhance the activity of glucocerebrosidase.
 17. The method of claim 16, wherein the lysosomal glucocerebrosidase is a mutant form of glucocerebrosidase which is present in patients with Gaucher disease.
 18. The method of claim 17, wherein the cell is a human cell.
 19. The method of claim 18 wherein the cell is from a patient with Gaucher disease.
 20. The method of claim 19, wherein the mutant glucocerebrosidase results from a homozygous mutation in the glucocerebrosidase gene.
 21. The method of claim 17, wherein the mutant form of glucocerebrosidase mutation is N370S.
 22. The method of claim 17, wherein the isofagomine compound is isofagomine.
 23. The method of claim 17, wherein the isofagomine compound is N-dodecyl-isofagomine.
 24. The method of claim 17, wherein the isofagomine compound is N-butyl-isofagomine.
 25. The method of claim 17 wherein the isofagomine compound is N-(3-cyclohexylpropyl)-isofagomine.
 26. The method of claim 17, wherein the isofagomine compound is N-(3-phenylpropyl)-isofagomine.
 27. The method of claim 17, wherein the isofagomine compound is N-[(2E,6Z,1OZ)-3,7,11-trimethyldodecatrienyl]-isofagomine.
 28. The method of claim 22, wherein the glucocerebrosidase activity is enhanced by about between 55–80% compared to activity of a mutant glucocerebrosidase in a cell not contacted with isofagomine.
 29. The method of claim 24, wherein the glucocerebrosidase activity is enhanced by about between 56–73% compared to activity of mutant glucocerebrosidase in a cell not contacted with N-butyl-isofagomine.
 30. The method of claim 25, wherein the glucocerebrosidase activity is enhanced by about between 47–106% compared to activity of mutant glucocerebrosidase in a cell not contacted with N-(3-cyclohexylpropyl)-isofagomine.
 31. The method of claim 26, wherein the glucocerebrosidase activity is enhanced by about between 50–54% compared to activity of mutant glucocerebrosidase in a cell not contacted with N-(3-phenylpropyl)-isofagomine.
 32. The method of claim 27, wherein the glucocerebrosidase activity is enhanced by about 43% compared to activity of mutant glucocerebrosidase in a cell not contacted with N-[(2E,6Z,10Z)-3,7,11-trimethyldodecatrienyl]-isofagomine.
 33. A method for treating Gaucher disease, which method comprises administering to an individual in need thereof an amount of isofagomine effective to treat Gaucher disease. 